B5 水光錠
B5 水光錠 : Product registered in Taiwan. This registration does not constitute authorisation for sale in France or the European Union. It does not demonstrate the safety or efficacy of the product.
TFDA, Taiwan tablets, capsules and medical nutrition registers, retrieved 27 October 2026.
Taiwan Food and Drug Administration (TFDA), Open Government Data License, version 1.0
- Registration number
- 1149037100
- Chinese name
- B5 水光錠
- English name
- B5 HYDRO GLOW TABLET
- Type
- Imported tablets and capsules
- Published status
- Status not provided in this export; the validity date is shown separately
- Licence holder
- 達爾膚生醫科技股份有限公司
- Registration date
- 2025-08-08
- Published validity end
- 2030-08-08
The foreign register category does not determine the regulatory category of the product in France.
French and European references for recognised ingredients
- À vérifier
The composition lists additive E171 (titanium dioxide), removed from the list of additives allowed in food, supplements included: since 7 August 2022, a supplement containing it can no longer be placed on the market in the Union.
règlement (UE) 2022/63. Regulation (EU) 2022/63: titanium dioxide (E171) removed from the food additives allowed in the EU, retrieved 23 October 2026.
Unidentified ingredients are not assessed. The absence of a signal does not establish product compliance.
Published composition
| Published ingredient | Published text and quantity | Identified nutrient or substance |
|---|---|---|
| MILK LIPID CONCENTRATE (CONTAIN CERAMIDES) | MILK LIPID CONCENTRATE (CONTAIN CERAMIDES) | Not identified |
| CALCIUM PANTOTHENATE | CALCIUM PANTOTHENATE | Acide pantothénique (vitamine B5) |
| DEXTRIN | DEXTRIN | Not identified |
| MICROCRYSTALLINE α-CELLULOSE | MICROCRYSTALLINE α-CELLULOSE | Not identified |
| CALCIUM CARBOXYMETHYL CELLULOSE | CALCIUM CARBOXYMETHYL CELLULOSE | Not identified |
| MAGNESIUM STEARATE | MAGNESIUM STEARATE | Not identified |
| SILICON DIOXIDE | SILICON DIOXIDE | Not identified |
| HYDROXYPROPYL METHYLCELLULOSE | HYDROXYPROPYL METHYLCELLULOSE | Not identified |
| WHITE COATING INGREDIENT (TABSHIELD) | WHITE COATING INGREDIENT (TABSHIELD) | Not identified |
| TITANIUM DIOXIDE | TITANIUM DIOXIDE | Not identified |
| TRIACETIN | TRIACETIN | Not identified |
| MIXED PREPARATION [CMC-NA (CARBOXYMETHYLCELLULOSE SODIUM)] | MIXED PREPARATION [CMC-NA (CARBOXYMETHYLCELLULOSE SODIUM)] | Not identified |
| SODIUM CARBOXYMETHYL CELLULOSE | SODIUM CARBOXYMETHYL CELLULOSE | Not identified |
| MALTODEXTRIN | MALTODEXTRIN | Maltodextrine |
| GLUCOSE | GLUCOSE | Glucose |
| LECITHIN | LECITHIN | Not identified |
| SODIUM CITRATE | SODIUM CITRATE | Not identified |
| GLYCEROL | GLYCEROL | Glycérol |
The imported data provide no usable daily dosage. No daily dose is estimated and no comparison with dose limits is performed. A published quantity may refer to a preparation or an unspecified unit. Chinese names are retained without translation.
Original register data
View published fields and their variants
- Product name
- B5 水光錠
- Active ingredients
- MILK LIPID CONCENTRATE (CONTAIN CERAMIDES);;CALCIUM PANTOTHENATE;;DEXTRIN;;MICROCRYSTALLINE α-CELLULOSE;;CALCIUM CARBOXYMETHYL CELLULOSE;;MAGNESIUM STEARATE;;SILICON DIOXIDE;;HYDROXYPROPYL METHYLCELLULOSE;;WHITE COATING INGREDIENT (TABSHIELD);;HYDROXYPROPYL METHYLCELLULOSE;;TITANIUM DIOXIDE;;TRIACETIN;;MIXED PREPARATION [CMC-NA (CARBOXYMETHYLCELLULOSE SODIUM)];;SODIUM CARBOXYMETHYL CELLULOSE;;MALTODEXTRIN;;GLUCOSE;;LECITHIN;;SODIUM CITRATE;;GLYCEROL;;
- Valid until
- 1190808
- Registration number
- 1149037100
- Licence holder
- 達爾膚生醫科技股份有限公司
- Registration date
- 1140808
- Published reference
- DHC0B490371002
- Published English name
- B5 HYDRO GLOW TABLET
Official source
View the official register, number 1149037100
Taiwan Food and Drug Administration (TFDA), Open Government Data License, version 1.0
Open Government Data License, version 1.0
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.